Canonical Allele Identifier: CA3614699
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs772118724
ExAC: 6:1610801 C / T
gnomAD v2: 6-1610801-C-T
gnomAD v3: 6-1610566-C-T
gnomAD v4: 6-1610566-C-T
COSMIC: COSM6384018
MyVariant Identifiers: chr6:g.1610801C>T (hg19) chr6:g.1610566C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610566C>T , CM000668.2:g.1610566C>T GRCh38
NC_000006.11:g.1610801C>T , CM000668.1:g.1610801C>T GRCh37
NC_000006.10:g.1555800C>T NCBI36
NG_009368.1:g.5121C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.121C>T MANE Select ENSP00000493906.1:p.Pro41Ser
ENST00000380874.3:c.121C>T ENSP00000370256.2:p.Pro41Ser
NM_001453.2:c.121C>T NP_001444.2:p.Pro41Ser
NM_001453.3:c.121C>T MANE Select NP_001444.2:p.Pro41Ser
Search 100 bp 5'
Search 100 bp 3'